Clinical and Virological Outcomes of TB/HIV Coinfected Patients Treated With Dolutegravir-Based HIV Antiretroviral Regimens: Programmatic Experience From Botswana.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 10 2019
Historique:
pubmed: 25 7 2019
medline: 17 4 2020
entrez: 24 7 2019
Statut: ppublish

Résumé

Dolutegravir (DTG) has recently been recommended as a preferred first-line regimen for the treatment of new and treatment-experienced HIV-infected patients. However, potential drug interactions between DTG and rifampicin remain a clinical and public health concern. We analyzed HIV and Tuberculosis (TB) treatment outcomes of HIV-infected patients concomitantly receiving rifampicin- and DTG-based regimens under programmatic conditions in Botswana. The outcomes of interest were successful TB treatment and viral load suppression. We used multivariable logistic models to determine predictors for each outcome of interest. A total of 1225 patients were included in the analysis to evaluate predictors of successful TB outcome. Among patients on DTG and non-DTG regimens, 90.9% and 88.3% achieved favorable TB treatment outcomes, respectively. Of those who received DTG-based regimen; 44% received once-daily dosing and 53% twice-daily dosing. We found that DTG was associated with favorable TB treatment outcome (adjusted odds ratio = 1.56; 95% confidence interval = 1.06 to 2.31), after adjusting for age, gender, and CD4 cell counts. High rates of viral load suppression were found across all antiretroviral therapy (ART) regimen categories (>92% for all). We did not find an independent association between DTG and viral suppression after adjustment of other covariates. The use of DTG-based ART regimens in patients coinfected with TB and HIV lead to favorable TB and HIV treatment outcomes, comparable to those achieved with alternative ART regimens. Our results provide reassurance to TB and HIV programs about the overall programmatic concomitant use of these first-line treatment regimens for the management of HIV and TB coinfected patients.

Sections du résumé

BACKGROUND
Dolutegravir (DTG) has recently been recommended as a preferred first-line regimen for the treatment of new and treatment-experienced HIV-infected patients. However, potential drug interactions between DTG and rifampicin remain a clinical and public health concern.
METHODS
We analyzed HIV and Tuberculosis (TB) treatment outcomes of HIV-infected patients concomitantly receiving rifampicin- and DTG-based regimens under programmatic conditions in Botswana. The outcomes of interest were successful TB treatment and viral load suppression. We used multivariable logistic models to determine predictors for each outcome of interest.
RESULTS
A total of 1225 patients were included in the analysis to evaluate predictors of successful TB outcome. Among patients on DTG and non-DTG regimens, 90.9% and 88.3% achieved favorable TB treatment outcomes, respectively. Of those who received DTG-based regimen; 44% received once-daily dosing and 53% twice-daily dosing. We found that DTG was associated with favorable TB treatment outcome (adjusted odds ratio = 1.56; 95% confidence interval = 1.06 to 2.31), after adjusting for age, gender, and CD4 cell counts. High rates of viral load suppression were found across all antiretroviral therapy (ART) regimen categories (>92% for all). We did not find an independent association between DTG and viral suppression after adjustment of other covariates.
CONCLUSIONS
The use of DTG-based ART regimens in patients coinfected with TB and HIV lead to favorable TB and HIV treatment outcomes, comparable to those achieved with alternative ART regimens. Our results provide reassurance to TB and HIV programs about the overall programmatic concomitant use of these first-line treatment regimens for the management of HIV and TB coinfected patients.

Identifiants

pubmed: 31335593
doi: 10.1097/QAI.0000000000002126
pmc: PMC7794061
mid: NIHMS1532705
doi:

Substances chimiques

Anti-HIV Agents 0
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
Pyridones 0
dolutegravir DKO1W9H7M1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111-115

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI097045
Pays : United States

Références

Curr Opin HIV AIDS. 2017 Jul;12(4):414-422
pubmed: 28410249
Int J Antimicrob Agents. 2019 Aug;54(2):202-206
pubmed: 31002950
Br J Clin Pharmacol. 2015 Sep;80(3):502-14
pubmed: 25819132
Curr Opin HIV AIDS. 2017 Jul;12(4):355-358
pubmed: 28403028
Biochem Pharmacol. 2005 Sep 15;70(6):949-58
pubmed: 16054595
J Acquir Immune Defic Syndr. 2013 Jan 1;62(1):21-7
pubmed: 23075918

Auteurs

Chawangwa Modongo (C)

Botswana-UPenn Partnership, Global Health, University of Pennsylvania, Philadelphia.

Qiao Wang (Q)

Sue and Bill Gross School of Nursing, University of California Irvine.

Mbatshi Dima (M)

Botswana-UPenn Partnership, Global Health, University of Pennsylvania, Philadelphia.

Ogopotse Matsiri (O)

Botswana-UPenn Partnership, Global Health, University of Pennsylvania, Philadelphia.

Botshelo Kgwaadira (B)

Public Health Department, Botswana National Tuberculosis Program Ministry of Health and Wellness, Gaborone, Botswana.

Goabaone Rankgoane-Pono (G)

Public Health Department, Botswana National Tuberculosis Program Ministry of Health and Wellness, Gaborone, Botswana.

Sanghyuk S Shin (SS)

Sue and Bill Gross School of Nursing, University of California Irvine.

Nicola M Zetola (NM)

Department of Radiation Oncology, University of Pennsylvania Philadelphia, PA.

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Classifications MeSH